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Rh(I)-catalyzed asymmetric 1,2-addition to α-diketones with chiral sulfur-alkene hybrid ligands.

Organic letters (2012-01-12)
Xiangqing Feng, Yanzhao Nie, Jing Yang, Haifeng Du
RESUMO

This paper describes a Rh(I)-catalyzed highly efficient and enantioselective 1,2-addition of arylboronic acids to α-diketones with the use of a simple sulfur-alkene hybrid ligand. With as low as a 0.1 mol % catalyst loading, a variety of optically active α-hydroxyketones can be furnished in high yields with excellent ee's.

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Sigma-Aldrich
trans-2-Phenylvinylboronic acid, 97%